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Updated: Jan 31, 2026

Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
Published on: November 29, 2018
Trideuteromethylation Enabled by a Sulfoxonium Metathesis Reaction
Zuyuan Shen1, Shilei Zhang2, Huihui Geng1
1State Key Laboratory of Bioengineering Reactor, and Shanghai Key Laboratory of New Drug Design, School of Pharmacy , East China University of Science & Technology , Shanghai 200237 , China.
Abstract:
A conceptually novel sulfoxonium metathesis reaction between TMSOI and cost-effective DMSO- d6 is developed for the efficient generation of a new trideuteromethylation reagent TDMSOI. The new reagent TDMSOI is produced highly efficiently by simply heating a mixture of TMSOI and DMSO- d6 and directly used for subsequent trideuteromethylation in a "one-pot" operation. The preparative power of the new versatile reagent and the "one-pot" protocol is demonstrated by its use to install the -CD3 moiety into broad functionalities including phenols, thiophenols, acidic amines, and enolizable methylene units in high yield and at a useful level of deuteration (>87% D).
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